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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2015 | 1 |
2021 | 2 |
2024 | 0 |
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Effects of Recombinant Human Growth Hormone Treatment, Depending on the Therapy Start in Different Nutritional Phases in Paediatric Patients with Prader-Willi Syndrome: A Polish Multicentre Study.
J Clin Med. 2021 Jul 19;10(14):3176. doi: 10.3390/jcm10143176.
J Clin Med. 2021.
PMID: 34300343
Free PMC article.
Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader-Willi Syndrome.
Lecka-Ambroziak A, Wysocka-Mincewicz M, Doleżal-Ołtarzewska K, Zygmunt-Górska A, Żak T, Noczyńska A, Birkholz-Walerzak D, Stawerska R, Hilczer M, Obara-Moszyńska M, Rabska-Pietrzak B, Gołębiowska E, Dudek A, Petriczko E, Szalecki M, On Behalf Of The Polish Coordination Group For rhGH Treatment.
Lecka-Ambroziak A, et al. Among authors: dudek a.
Diagnostics (Basel). 2021 Apr 28;11(5):798. doi: 10.3390/diagnostics11050798.
Diagnostics (Basel). 2021.
PMID: 33925106
Free PMC article.
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Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands.
Kumorowicz-Czoch M, Madetko-Talowska A, Dudek A, Tylek-Lemanska D.
Kumorowicz-Czoch M, et al. Among authors: dudek a.
J Pediatr Endocrinol Metab. 2015 Jul;28(7-8):735-43. doi: 10.1515/jpem-2014-0310.
J Pediatr Endocrinol Metab. 2015.
PMID: 25720050
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